Clinical Research Associate II in London
Clinical Research Associate II

Clinical Research Associate II in London

London Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Manage clinical research sites and ensure successful study life cycles from start to finish.
  • Company: Join a rapidly growing global Contract Research Organisation focused on innovative therapies.
  • Benefits: Enjoy a car allowance, bonus, remote work, and extensive training opportunities.
  • Why this job: Make a real impact in cutting-edge research while advancing your career in a supportive environment.
  • Qualifications: Bachelor's in health-related field and at least 2 years of CRA experience required.
  • Other info: Promote up to 4 times a year with dedicated admin support for a balanced workload.

The predicted salary is between 36000 - 60000 £ per year.

Location: Remote in England

Additional Benefits: Car allowance (or company car) and bonus

Company: Global CRO

RBW Consulting is thrilled to present an exciting opportunity on behalf of one of our esteemed clients. As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of studies, including cutting-edge research in advanced therapies such as CAR-T.

Join a highly experienced team dedicated to excellence in clinical research. In this role, you will benefit from a supportive management team committed to your professional growth. They provide clear guidance on the skills needed for advancement and offer fluid career development opportunities across various departments. This company prioritises quality over metrics and is currently generating significant excitement within their UK team.

Key accountabilities:
  • Autonomy of investigator sites with full responsibility for the successful management of sites through study life cycle (start-up to close-out);
  • Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
  • Prepare accordingly and attend investigator meetings, coordinating timely delivery and subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues;
  • Perform source document verification and case report form review;
  • Perform regulatory document review;
  • Perform adverse event and serious adverse event reporting and follow-up;
  • Assess patient recruitment and retention.
Qualifications:
  • Bachelor of Science in health-related field (or equivalent)
  • Proven CRA experience; 2 years minimum
Why Join?
  • Supportive Environment: Build strong relationships with a transparent management team focused on your development.
  • Innovative Approach: Work with a company that embraces a 360 monitoring approach and leverages AI to enhance efficiency and save time.
  • Results-Driven KPIs: Our client's key performance indicators are centered around tangible study outcomes, such as patient recruitment, visit reports, and resolving site issues.
  • Administrative Support: Dedicated admin staff to help with site management tasks, helping to maintain a balanced workload.
  • Training: Extensive training and buddy system in place.
  • Career Growth: promotion opportunities up to 4 times a year.
  • Therapy Areas: Access to mixed therapy areas, including advanced therapies like CAR-T.

To apply, please click ‘apply’ or contact Joe Pearce for any further information.

About RBW Consulting: RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients. We give back by playing an active role in funding initiatives that change lives. We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.

We are an equal opportunities Recruitment Business and Agency. RBW Consulting is an equal opportunity workplace. We prioritise talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.

Clinical Research Associate II in London employer: RBW Consulting

Join a dynamic and rapidly growing Contract Research Organization that prioritises quality and innovation in clinical research. With a strong focus on employee development, you will benefit from a supportive management team, extensive training, and clear pathways for career advancement, all while working remotely in England. Enjoy unique perks such as a car allowance, bonus opportunities, and the chance to engage in cutting-edge studies across diverse therapeutic areas, including advanced therapies like CAR-T.
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Contact Detail:

RBW Consulting Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Research Associate II in London

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a job that’s perfect for you.

✨Tip Number 2

Prepare for interviews by researching the company and its recent projects. Show them you’re genuinely interested in their work, especially in advanced therapies like CAR-T. Tailor your answers to reflect how your experience aligns with their goals.

✨Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors to boost your confidence. Focus on articulating your CRA experience clearly, especially around site management and patient recruitment.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re here to support you every step of the way in landing that dream job!

We think you need these skills to ace Clinical Research Associate II in London

Clinical Research Experience
Site Management
Feasibility Assessment
Monitoring Visits
Regulatory Document Review
Adverse Event Reporting
Source Document Verification
Case Report Form Review
Patient Recruitment Strategies
Communication Skills
Team Collaboration
Problem-Solving Skills
Attention to Detail
Time Management

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate II role. Highlight relevant experience, especially in managing investigator sites and conducting feasibility studies. We want to see how your background aligns with our needs!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how you can contribute to our supportive environment. We love seeing genuine enthusiasm for the role.

Showcase Your Skills: Don’t forget to highlight your skills in monitoring, regulatory document review, and patient recruitment. We’re looking for someone who can hit the ground running, so make sure we know what you bring to the table!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team!

How to prepare for a job interview at RBW Consulting

✨Know Your Stuff

Make sure you brush up on the latest trends in clinical research, especially around advanced therapies like CAR-T. Familiarise yourself with the study life cycle and be ready to discuss your previous experiences managing investigator sites.

✨Showcase Your Autonomy

This role requires a lot of independence, so be prepared to share examples of how you've successfully managed sites on your own. Highlight any challenges you've faced and how you overcame them to demonstrate your problem-solving skills.

✨Ask Insightful Questions

Prepare thoughtful questions about the company’s approach to patient recruitment and retention, as well as their use of AI in monitoring. This shows your genuine interest in their innovative methods and helps you assess if it’s the right fit for you.

✨Emphasise Career Growth

Since this company values professional development, talk about your career aspirations and how you see yourself growing within the organisation. Mention any specific skills you want to develop that align with their training opportunities.

Clinical Research Associate II in London
RBW Consulting
Location: London

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